Tanaka K, Okazaki K, Okazaki N, Ueda T, Sugiyama A, Nojima H, Okayama H
Department of Molecular Genetics, Osaka University, Japan.
EMBO J. 1992 Dec;11(13):4923-32. doi: 10.1002/j.1460-2075.1992.tb05599.x.
We have isolated a new cell division cycle gene (res1+) required for entry into S phase, as a multicopy dual suppressor of the pat1 and cdc10 mutants of the fission yeast Schizosaccharomyces pombe. The res1+ gene specifies a 72 kDa protein with two copies of the cdc10/SWI6 motif. A disruptant of res1+ grows poorly at 30 degrees C with severe heat- and cold-sensitivities, and completely arrests in G1 at 36 degrees C and 23 degrees C. The arrested disruptant retains a full conjugation ability. In addition to the cdc10/SWI6 motif, Res1 and SWI4 proteins share a remarkable homology in their amino-terminal region, whereas Cdc10 and SWI6 do so in their carboxy-terminal region. Moreover, the amino-terminal region is essential for the function of Res1 as it is for the function of SWI4. Furthermore, analogous to the relationship of SWI4 to SWI6, the res1+ gene effectively rescues cdc10 mutants, but the cdc10+ gene cannot rescue the res1- phenotype. Thus, striking similarities exist in both structural and functional relationships between Res1 and SWI4, and between Cdc10 and SWI6. In view of the fact that SWI4 and SWI6 form a transcription factor complex and activate promoters containing the SWI4/SWI6 dependent cell-cycle box, Res1 might be a putative association partner of Cdc10 which appears to be involved at least in the activation of promoters containing a MluI cell-cycle box.
我们分离出了一个进入S期所需的新细胞分裂周期基因(res1+),它是粟酒裂殖酵母Schizosaccharomyces pombe的pat1和cdc10突变体的多拷贝双重抑制子。res1+基因编码一种72 kDa的蛋白质,含有两个cdc10/SWI6基序拷贝。res1+缺失突变体在30℃下生长不良,对高温和低温敏感,在36℃和23℃时完全停滞在G1期。停滞的缺失突变体保留了完整的接合能力。除了cdc10/SWI6基序外,Res1和SWI4蛋白在其氨基末端区域具有显著的同源性,而Cdc10和SWI6在其羧基末端区域具有同源性。此外,氨基末端区域对Res1和SWI4的功能都是必需的。此外,类似于SWI4与SWI6的关系,res1+基因能有效拯救cdc10突变体,但cdc10+基因不能拯救res1-表型。因此,Res1与SWI4之间以及Cdc10与SWI6之间在结构和功能关系上都存在显著相似性。鉴于SWI4和SWI6形成转录因子复合物并激活含有SWI4/SWI6依赖性细胞周期框的启动子,Res1可能是Cdc10的假定结合伙伴,而Cdc10似乎至少参与了含有MluI细胞周期框的启动子的激活。